Exosomes are cell-secreted vesicles secreted by a majority of cells and, hence, populating most of the biological fluids, namely blood, tears, sweat, swab, urine, breast milk, etc. They vary vastly in size and density and are influenced by age, gender and diseases. The composition of exosomes includes lipids, DNA, proteins, and coding and noncoding RNA. There is a significant interest in selectively isolating small exosomes (≤50 nm) from human serum to investigate their role in different diseases and regeneration. However, current techniques for small exosome isolation/purification are time-consuming and highly instrument-dependent, with limited specificity and recovery. Thus, rapid and efficient methods to isolate them from bio fluids are strongly needed for both basic research and clinical applications. In the present work, we explored the application of a bench-top centrifuge for isolating mostly the small exosomes (≤50 nm). This can be achieved at low g-force by adding additional weight to the exosomes by conjugating them with citrate-capped gold nanoparticles (CGNP). CGNPs were functionalized with polyethylene glycol (PEG) to form PEGylated GNP (PGNP). EDC/SNHS chemistry is used to activate the –COOH group of the PEG to make it suitable for conjugation with antibodies corresponding to exosomal surface proteins. These antibody-conjugated PGNPs were incubated with the serum to form PGNP-exosome complexes which were separated directly by centrifugation at a low g-force of 7000× g. This makes this technique efficient compared to that of standard ultracentrifugation exosome isolation (which uses approximately 100,000× g). Using the technique, the exosome isolation from serum was achieved successfully in less than two hours. The purification of small exosomes, characterized by the presence of CD63, CD9 and CD81, and sized between 20 nm to 50 nm, was confirmed by western blot, dynamic light scattering (DLS), transmission electron microscopy (TEM) and nanoparticle tracking analyser (NTA).

An ultralow power suspended gas sensor with in-plane heater and nano gap sensor electrodes is presented. The heater and sensing electrodes, separated by 1-μm air gap, are processed using single lithography step with standard micro-fabrication techniques. Controlled electromigration is used to create a nanogap in the middle of the sensing electrode. The sol-gel grown ZnO is dispensed using a picoliter dispenser to bridge the nanogap electrode, created by electromigration, to get required metal oxide film as a sensing element. The gap between the electrode and heater is optimized by electrothermal simulation to obtain desired temperature profile on ZnO. The resulting device exhibits excellent sensing performance for hydrogen (~86% at 20 ppm) at 0.5 mW. A detailed characterization was carried out to analyze the performance of the device. This unique, in-plane structure is superior compared with the conventional out of plane structure in terms of the power efficiency and ease of processing.

Exosomes, whose mean diameter ranges from 20 nm to 200 nm, are cell-secreted vesicles and are abundant in most biological fluids, such as blood, urine, tears, sweat, breast milk, etc. Exosomal size variations and their composition can be attributed to several factors, such as age, gender and disease conditions of the individual. Existing techniques, such as ultracentrifugation and density gradient ultracentrifugation, for exosome isolation are instrument-dependent, time-consuming and lack specificity. In the present work, a gold-nanoparticle (GNP)-coated silicon (Si) wafer, functionalized with polyethylene glycol (PEG) was used for conjugation with anti-CD63 antibody via EDC NHS chemistry and incubated with serum to immobilize the exosomes on the Si surface. The surface-immobilized exosomes were eluted and quantified by a nanoparticle tracking analyzer (NTA). It was observed that an increase in GNP density on the Si wafer increases the size range and total number of exosomes that are being isolated. Western blotting performed for proteins such as HSP 70 and calnexin confirmed the immobilization and elution of exosomes. The proposed technique can be used as an alternative to existing techniques, as it has several benefits such as reusability of the Si surface for several isolations, minimal instrumental requirement, isolation of exosomes in two hours and compatibility with the microfluidic platform, making the technique suitable for real-time application. The proposed method could be useful in isolating a specific subrange of exosomes by altering the size of the GNP used for coating the Si wafer.

Tunable conductivity of graphene, makes it a promising material for metamaterials. There are various graphene tunable metamaterial absorbers in the mid-infrared region, whose absorption spectrum can be dynamically tuned by varying the Fermi potential of graphene. However, graphene absorbers working in the low mid-infrared region (4–7 μm) has limited tuning. In this work, the spectral tuning efficiency of a graphene based metal disc pattern and a graphene ribbon pattern metamaterial absorber is studied using FDTD simulation. The tunability in absorption spectrum achieved by metal disc absorber is 2–4%, which increased to 5–20% for graphene ribbon absorber with more than 85% absorption rate. Thus, the graphene pattern absorber significantly improves the tunability and provides broad tuning in 4–7 μm wavelength range. However, the graphene ribbon absorber is polarization dependent due to its non-symmetric shape. Hence, a new type of nano square hole (NSH) graphene absorber is proposed, which can easily be externally biased and provide polarization independent absorption. The NSH graphene absorber has wide tunability of 5–20% and high absorption rate of 85% similar to the graphene ribbon absorber. These results are very helpful to design tunable sensors and multispectral devices for gas sensor and biosensor applications.

It is important to isolate exosomes (<150 nm) from biofluid for diagnosis or prognosis purposes, followed by sensing of exosomal proteins. In the present work, exosomes are isolated from human serum by immobilizing on a Screen-Printed Electrode (SPE) followed by electric field lysis and electrochemical impedance spectroscopy (EIS)-based sensing of relevant exosomal proteins (HSP70 and HER2). Upon immobilization of exosomes on the surface, the role of different electrical signals (sinusoidal and square wave) in the lysis of exosomes was studied by varying the frequency and voltage. HSP70 was used for EIS to determine the optimal voltage and frequency for lysing the exosomes. It was observed that the low frequencies and, specifically, sinusoidal signals are ideal for lysing exosomes as compared to square signals. The relative quantity of HSP70 obtained by lysing with different voltages (sinusoidal waveform) was compared using Western blotting. After electric field lysis of the exosome with an optimized signal, HER2, a breast cancer biomarker, was detected successfully from serum by EIS. In the proposed technique, 3.5 × 10⁸ exosomes/mL were isolated from serum. With the limit of detection of 10 pg, the designed cell showed a linear detection of HER2 from 0.1 ng to 1 µg. It was observed from the results that the electric field lysis of exosomes not only plays a significant role in releasing the cargo protein but also improves the sensing of surface proteins associated with exosomes.

A chemical method for preparing CuI thin films by iodination of solution grown Cu₂S films is described. X-ray characterization identifies γ-CuI and suggest that the films are polycrystalline in nature. SEM reveals a granular film morphology. Optical studies show that the band gap of the material is 2.93 eV. The sheet resistance of the films is in the range 1 to 3 k Ω/sq.